G.A. Molfetta
Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil
Familial hypercholesterolemia (FH) is a dominant, autosomal disease characterized by high LDL levels in blood plasma, and is caused by a defect in the gene encoding the LDL receptor (LDLR). The clinical diagnosis is based on personal and familial history, physical examination findings, and measures of high LDL cholesterol concentrations. LDLR is a cell-surface glyco.. Read More»
Genet. Mol. Res. 16(3): gmr16039226
DOI: 10.4238/gmr16039226
Microarray profiles of ex vivo expanded hematopoietic stem cells show induction of genes involved in noncanonical Wnt signaling
The low number of hematopoietic stem cells (HSC) in umbilical cord blood (UCB) is directly related to increased risk of transplant failure. Effective ex vivo expansion of HSC has been tried for many years, with conflicting results because of the inability to reproduce in vitro HSC proliferation in the same way it occurs in vivo. We compared freshly isolated HSC with their expanded counterparts .. Read More»
Genet. Mol. Res. 12(2): 2013.May.15.1
DOI: 10.4238/2013.May.15.1
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